Our mission is to improve the health prospects of women living with
lymphangioleiomyomatosis (LAM).
LAM Australia Research Alliance is a not-for-profit organisation run wholly by volunteers.
Our mission is to improve the health prospects of women living with
ABOUT US
- Funding research to find a cure for LAM
- Raising awareness of LAM
- Supporting women living with LAM
DOCTORS WITH LAM EXPERTISE
PATIENT SUPPORT CONTACTS FOR WOMEN NEWLY DIAGNOSED WITH LAM
NEWS
Please join us for the Annual General Meeting on Tuesday 11 August 2020 at 18.00 AEST. Our AGM will be followed by a talk by Prof Allan Glanville, world clinical authority on the treatment of LAM. Our talk will be held on Zoom. If you have not received an email already about the AGM, pleased email us at admin@lamaustralaia.org.au to register.
Our Supporters
OUR TEAM
PATRON
Dr Linda Friedland
MEDICAL & SCIENTIFIC ADVISORY PANEL
Prof David Sonnabend (Convenor)
Prof Judith Black AO
Dr Tamera Corte
Prof Allan Glanville
Dr Jeffrey Lindenmayer
A/Prof Mervyn Merrilees
Dr Helen Whitford
A/Prof Deborah Yates
EXECUTIVE
President: Dr Brian Oliver
Treasurer: Michael Neustein
COMMITTEE
Pat Evans
Melanie Hawyes
Faith Wieland
Yasuko Wilson
Public Officer: Peter Kelso
Hon Auditor: Peter Hersh, Logicca P/L
ACKNOWLEDGEMENTS
LAM Australia thanks the professionals who work pro bono for this not-for-profit organisation.
We highly recommend the services of:
Karen Riethmuller, KGR Design
Peter Hersh, Loggica Pty Ltd
Rohan Napier, RedRo Design
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© 2015 Copyright LAM Australia. All rights reserved
RESEARCH GIVES HOPE TO WOMEN WITH LAM